Clarin‐1 expression in adult mouse and human retina highlights a role of Müller glia in Usher syndrome

Usher syndrome type 3 (USH3) is an autosomal recessively inherited disorder caused by mutations in the gene clarin‐1 (CLRN1), leading to combined progressive hearing loss and retinal degeneration. The cellular distribution of CLRN1 in the retina remains uncertain, either because its expression level...

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Detalles Bibliográficos
Autores principales: Xu, Lei, Bolch, Susan N, Santiago, Clayton P, Dyka, Frank M, Akil, Omar, Lobanova, Ekaterina S, Wang, Yuchen, Martemyanov, Kirill A, Hauswirth, William W, Smith, W Clay, Handa, James T, Blackshaw, Seth, Ash, John D, Dinculescu, Astra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2019
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003947/
https://www.ncbi.nlm.nih.gov/pubmed/31625146
http://dx.doi.org/10.1002/path.5360

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003947/
https://www.ncbi.nlm.nih.gov/pubmed/31625146
http://dx.doi.org/10.1002/path.5360

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